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Siemens

FDA UDI

Class II (US FDA UDI)

by WS Audiology USA, Inc.

Identity

Trade Name
Siemens FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
SIEMENS HA ORION RIC SLV Hearing Aid FDA UDI
Model / Reference
HA ORION RIC SLV FDA UDI
Description
SIEMENS HA ORION RIC SLV Hearing Aid FDA UDI

Identifiers

Catalog Number
10822523 FDA UDI
Primary DI / UDI-DI
04046355611580 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Air-conduction hearing aid, behind-the-ear FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3305 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Siemens by WS Audiology USA, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 188ebb86-77b8-4b3a-a770-955483de5408 36 fields · synced May 30, 2026